510(k) K123497 ยท MRW System, Facet Screw Spinal Device
FACET SCREW SYSTEM
| Applicant | Facet-Link, Inc., Philedelphia PA, US |
| Decision | Substantially Equivalent, Feb 28, 2013 |
| Received | Nov 13, 2012 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K123497
No recall in the FDA data names this 510(k).
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.